Canonical Allele Identifier: CA349894345

Gene: HIBCH

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190213029T>A , CM000664.2:g.190213029T>A	GRCh38
NC_000002.11:g.191077755T>A , CM000664.1:g.191077755T>A	GRCh37
NC_000002.10:g.190786000T>A	NCBI36
NG_017062.1:g.112017A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014362.4:c.938A>T MANE Select	NP_055177.2:p.Gln313Leu
ENST00000359678.10:c.938A>T MANE Select	ENSP00000352706.5:p.Gln313Leu
NM_014362.3:c.938A>T	NP_055177.2:p.Gln313Leu
NM_198047.2:c.938A>T	NP_932164.1:p.Gln313Leu
NM_198047.3:c.938A>T	NP_932164.1:p.Gln313Leu
ENST00000359678.9:c.938A>T	ENSP00000352706.5:p.Gln313Leu
ENST00000392332.7:c.938A>T	ENSP00000376144.3:p.Gln313Leu
ENST00000409820.2:c.278A>T	ENSP00000387098.2:p.Gln93Leu
ENST00000410045.5:c.269A>T	ENSP00000386274.1:p.Gln90Leu
ENST00000416732.5:c.191A>T	ENSP00000399263.1:p.Gln64Leu
ENST00000486981.1:n.207A>T
ENST00000489147.1:n.3081A>T
ENST00000622246.4:c.920A>T	ENSP00000481055.1:p.Gln307Leu
XM_011510953.1:c.938A>T	XP_011509255.1:p.Gln313Leu
XM_011510953.2:c.938A>T	XP_011509255.1:p.Gln313Leu
XM_011510954.1:c.440A>T	XP_011509256.1:p.Gln147Leu
XR_922903.1:n.1182A>T
XR_922903.2:n.1001A>T